Published online May 26, 2019. doi: 10.4330/wjc.v11.i5.137
Peer-review started: February 22, 2019
First decision: March 15, 2019
Revised: April 2, 2019
Accepted: May 22, 2019
Article in press: May 22, 2019
Published online: May 26, 2019
Previous studies have established a role of gout in predicting risk and prognosis of cardiovascular diseases. However, large-scale data on the impact of gout on inpatient outcomes of acute coronary syndrome (ACS)-related hospitalizations and post-revascularization is inadequate.
To evaluate the impact of gout on in-hospital outcomes of ACS hospitalizations, subsequent healthcare burden and predictors of post-revascularization inpatient mortality.
We used the national inpatient sample (2010-2014) to identify the ACS and gout-related hospitalizations, relevant comorbidities, revascularization and post-revascularization outcomes using the ICD-9 CM codes. A multivariable analysis was performed to evaluate the predictors of post-revascularization in-hospital mortality.
We identified 3144744 ACS-related hospitalizations, of which 105198 (3.35%) also had gout. The ACS-gout cohort were more often older white males with a higher prevalence of comorbidities. Coronary artery bypass grafting was required more often in the ACS-gout cohort. Post-revascularization complications including cardiac (3.2% vs 2.9%), respiratory (3.5% vs 2.9%), and hemorrhage (3.1% vs 2.7%) were higher whereas all-cause mortality was lower (2.2% vs 3.0%) in the ACS-gout cohort (P < 0.001). An older age (OR 15.63, CI: 5.51-44.39), non-elective admissions (OR 2.00, CI: 1.44-2.79), lower household income (OR 1.44, CI: 1.17-1.78), and comorbid conditions predicted higher mortality in ACS-gout cohort undergoing revascularization (P < 0.001). Odds of post-revascularization in-hospital mortality were lower in Hispanics (OR 0.45, CI: 0.31-0.67) and Asians (OR 0.65, CI: 0.45-0.94) as compared to white (P < 0.001). However, post-operative complications significantly raised mortality odds. Mean length of stay, transfer to other facilities, and hospital charges were higher in the ACS-gout cohort.
Although gout was not independently associated with an increased risk of post-revascularization in-hospital mortality in ACS, it did increase post-revascularization complications.
Core tip: Previous studies have established a role of gout in predicting risk and prognosis of cardiovascular diseases. However, large-scale data on the impact of gout on inpatient outcomes of acute coronary syndrome (ACS)-related hospitalizations and post-revascularization is inadequate. In this largest nationwide cohort, we identified 3144744 ACS-related hospitalizations, of which 105198 (3.35%) also had gout. Coronary artery bypass grafting was required more often in the ACS-gout cohort. Post-revascularization (percutaneous coronary intervention/coronary artery bypass grafting) complications including cardiovascular (3.2% vs 2.9%), respiratory (3.5% vs 2.9%), and hemorrhage (3.1% vs 2.7%) were higher and raised the mortality odds whereas all-cause mortality was lower (2.2% vs 3.0%) in the ACS-gout cohort. Mean length of stay, transfers and hospital charges were higher in the ACS-gout cohort.
- Citation: Desai R, Parekh T, Goyal H, Fong HK, Zalavadia D, Damarlapally N, Doshi R, Savani S, Kumar G, Sachdeva R. Impact of gout on in-hospital outcomes of acute coronary syndrome-related hospitalizations and revascularizations: Insights from the national inpatient sample. World J Cardiol 2019; 11(5): 137-148
- URL: https://www.wjgnet.com/1949-8462/full/v11/i5/137.htm
- DOI: https://dx.doi.org/10.4330/wjc.v11.i5.137
Acute coronary syndrome (ACS) comprises a range of diseases including unstable angina (UA), non-ST segment elevation myocardial infarction, and acute ST-elevation myocardial infarction (STEMI)[1]. It is one of the major causes of mortality around the world. Several independent predictors including advanced age, gender, history of diabetes or hypertension, obesity, and socioeconomic status have been determined for the unfavorable outcomes and rise in the overall mortality in ACS patients[2,3]. Gout is a common inflammatory disease associated with hyperuricemia and has shown to be associated with almost 410% increase in the hospitalizations in the last two decades in the United States[4]. The clinical evidence has shown that uric acid (UA) may have a pro-inflammatory effect on the vascular cells contributing to the negative effects of hyperuricemia in cardiovascular diseases (CVD) including ACS[5,6]. Previous studies have also suggested that gout patients have two to five-fold higher mortality risk in patients with CVD[7,8]. Recent studies have also established the crucial role of high UA levels in predicting the higher odds of MI and subsequent in-hospital mortality in ACS and STEMI hospitalizations[9,10]. Furthermore, microvasculature is becoming a key prognostic factor in patients undergoing percutaneous coronary intervention (PCI) since UA has been found to induce microvascular lesions, accounting for vascular dementia and allograft vasculopathy post-cardiac transplantation[11]. While quick restoration of blood flow through an infarct-related artery is important, the presence of distal microvascular disease can result in impaired myocardial flow leading to an increased risk of major adverse cardiac events after acute MI[12,13]. Nevertheless, the relationship between gout and healthcare resource utilization and post-revascularization outcomes in ACS hospitalizations has not been previously studied on a large scale in the United States. Therefore, in this retrospective population-based study, we aim to evaluate the impact of gout on the in-hospital outcomes of ACS hospitalizations, subsequent healthcare burden and predictors of post-revascularization inpatient mortality using the largest nationwide cohort from January 2010 through December 2014.
The study cohort was derived from the national inpatient sample (NIS) database from January 2010 through December 2014, which is a part of the Healthcare Cost and Utilization Project held by the Agency for Healthcare Research and Quality (AHRQ). The NIS is the largest publicly accessible all-payer inpatient database in the United States and incorporates diverse identifiers for the hospitalization and clinical data for each visit including up to 25 discharge diagnoses and 15 procedures[14]. It includes discharge statistics from 20% inpatient discharges of all non-federal United States hospital facilities (not including rehabilitation and long-term acute care hospitals), disclosing up to 95% of hospital releases across the country. Nationwide assessments were generated utilizing discharge weights provided by AHRQ.
All ACS-related adult hospitalizations were recognized by applying International Classification of Diseases, Ninth Revision; Clinical Modification (ICD-9-CM) codes 410.1x and 411.1 for the primary discharge diagnosis. These codes have been successfully utilized in earlier studies[15]. We then divided ACS population into the two cohorts: one who had baseline gout and another without gout by using ICD-9 CM codes 274.x or 274.xx in any of the secondary discharge diagnoses.
Patient and hospital-level variables including age, gender, race, median household income, primary payer, hospital location/teaching status, bed size, and regions were studied and compared between ACS hospitalizations with vs without gout. Underlying comorbid illnesses were also compared between the ACS population with vs without gout. Revascularization comprised of thrombolysis (ICD-9 CM diagnosis code V45.88 or procedure code 99.10), PCI (ICD-9 CM procedure codes 00.66, 36.01, 36.02, 36.05, 36.06, and 36.07, 17.55) OR CABG (ICD-9 CM procedure codes 36.10, 36.11, 36.12, 36.13, 36.14, 36.15, 36.16, 36.17, 36.19, 36.2, 36.3, 36.31, 36.32, 36.33, 36.34, 36.39). Since the NIS is an openly available database with de-identified data, our study was exempt from an Institutional Review Board authorization.
The primary outcomes of interest were all-cause in-hospital mortality, revascula-rization (thrombolysis, PCI or CABG) rates, discharge disposition, length of hospital stay (LOS), and total hospital charges (denotes the total amount payable for service rather than the actual payment received). The secondary outcomes were post-revascularization complications in ACS-hospitalizations including all-cause in-hospital mortality, hemorrhage, blood transfusion, hypotension/shock, cardiac complications, postoperative myocardial infarction, stroke, respiratory complications, gastrointestinal complications including gastrointestinal hemorrhage, acute kidney injury (AKI) requiring dialysis, urinary complications, postoperative infections, and predictors of in-hospital mortality. Comorbidities and postoperative complications were identifying from the secondary discharge diagnoses. The codes used in the study to identify comorbidities and post-revascularization complications are mentioned in Supplementary Table 1.
| Variables | Without gout(n = 3039546) | With gout(n = 105198) | P value |
| Age (yr) at hospitalization | < 0.001a | ||
| mean (± SD) | 66.9 (± 14.2) | 71.3 (± 12.5) | |
| 18-44 | 171857 (5.7) | 2337 (2.2) | |
| 45-64 | 1178621 (38.8) | 28567 (27.2) | |
| 65-84 | 1288783 (42.4) | 57054 (54.2) | |
| ≥ 85 | 400285 (13.2) | 17240 (16.4) | |
| Sex | < 0.001a | ||
| Male | 1830228 (60.2) | 77834 (74.0) | |
| Female | 1209120 (39.8) | 27355 (26.0) | |
| Race | < 0.001a | ||
| White | 2102509 (75.4) | 69431 (71.8) | |
| African American | 302121 (10.8) | 14798 (15.3) | |
| Hispanic | 218605 (7.8) | 4833 (5.0) | |
| Asian and Pacific Islander | 61156 (2.2) | 4799 (5.0) | |
| Native American | 16624 (0.6) | 394 (0.4) | |
| Others | 88091 (3.2) | 2477 (2.6) | |
| Admission type | < 0.001 | ||
| Non-elective | 2847182 (93.9) | 98886 (94.1) | |
| Elective | 185903 (6.1) | 6149 (5.9) | |
| Median household income percentile for patient's zip code1 | < 0.001a | ||
| 0-25th | 894564 (30.1) | 29758 (28.8) | |
| 26-50th | 807784 (27.2) | 26606 (25.8) | |
| 51-75th | 701363 (23.6) | 24152 (23.4) | |
| 76-100th | 566069 (19.1) | 22637 (21.9) | |
| Primary expected payer | < 0.001a | ||
| Medicare | 1709250 (56.4) | 72559 (69.1) | |
| Medicaid | 218428 (7.20) | 4232 (4.0) | |
| Private including HMO | 803459 (26.5) | 22757 (21.7) | |
| Self-pay/no charge/others | 301827 (10.0) | 5433 (5.2) | |
| Control/ownership of hospital | < 0.001a | ||
| Government, nonfederal | 305519 (10.1) | 9697 (9.3) | |
| Private, non-profit | 2258936 (74.7) | 81175 (77.4) | |
| Private, invest-own | 459942 (15.2) | 13962 (13.3) | |
| Bed size of hospital | 0.157 | ||
| Small | 351544 (11.6) | 12101 (11.5) | |
| Medium | 767625 (25.4) | 26387 (25.2) | |
| Large | 1905229 (63.0) | 66346 (63.3) | |
| Location/teaching status | < 0.001a | ||
| Rural | 312292 (10.3) | 10030 (9.6) | |
| Urban non-teaching | 1183544 (39.1) | 37858 (36.1) | |
| Urban teaching | 1528562 (50.5) | 56946 (54.3) | |
| Region of hospital | < 0.001a | ||
| Northeast | 575864 (18.9) | 19077 (18.1) | |
| Midwest | 705042 (23.2) | 24946 (23.7) | |
| South | 1219352 (40.1) | 39502 (37.5) | |
| West | 539288 (17.7) | 21672 (20.6) |
We integrated the discharge weights to unweighted records, to generate the national estimates. The missing data (< 10% for any variable) were omitted from the analysis. The baseline characteristics were compared amongst ACS patients with gout and without gout by applying Pearson’s Chi-square test for categorical and Student's t-test for the continuous variable where appropriate. We developed a two-step hierarchical multivariate logistic regression model to evaluate for the patient and hospital level components, and in-hospital outcomes such as in-hospital mortality and procedural complications related to the ACS. This model permitted us to represent the possible relationship of insights into each hospital visit. Both patient and hospital level components along with all relevant comorbidities were incorporated into the multivariable model to control confounders. In addition to unadjusted analysis, post-revascularization outcomes were also analyzed using a propensity score-matched analysis with a caliper width of 0.01 without replacement and adjusting for demographics and all relevant comorbid conditions (Supplementary Tables 2 and 3). A two-tailed P-value of < 0.5 was considered statistically significant. All statistical analyses were completed utilizing SPSS Statistics 24 (IBM Corp., Armonk, NY).
| Comorbidities | ACS + no gout | ACS + gout | P value |
| Alcohol abuse | 95449 (3.1) | 3768 (3.6) | < 0.001a |
| Deficiency anemias | 487126 (16.0) | 28065 (26.7) | < 0.001a |
| Rheumatoid arthritis/collagen vascular diseases | 72214 (2.4) | 3343 (3.2) | < 0.001a |
| Congestive heart failure | 24213 (0.8) | 811 (0.8) | 0.357 |
| Chronic pulmonary disease | 634046 (20.9) | 22789 (21.7) | < 0.001a |
| Coagulopathy | 152932 (5.0) | 7283 (6.9) | < 0.001a |
| Diabetes, uncomplicated | 911629 (30.0) | 36556 (34.7) | < 0.001a |
| Diabetes with chronic complications | 200881 (6.6) | 12597 (12.0) | < 0.001a |
| Drug abuse | 95449 (3.1) | 1519 (1.4) | < 0.001a |
| Hypertension | 75189 (2.5) | 87598 (83.3) | < 0.001a |
| Hypothyroidism | 2170519 (71.4) | 15366 (14.6) | < 0.001a |
| Liver disease | 334044 (11.0) | 2013 (1.9) | < 0.001a |
| Fluid and electrolyte disorders | 43749 (1.4) | 26081 (24.8) | < 0.001a |
| Other neurological disorders | 636496 (20.9) | 6138 (5.8) | < 0.001a |
| Obesity | 186097 (6.1) | 23082 (21.9) | < 0.001a |
| Peripheral vascular disorders | 443723 (14.6) | 16964 (16.1) | < 0.001a |
| Renal failure | 355484 (11.7) | 47359 (45.0) | < 0.001a |
| Valvular disease | 568903 (18.7) | 327 (0.3) | < 0.001a |
| Dyslipidemia | 7101 (0.2) | 74674 (71.0) | < 0.001a |
| Coronary atherosclerosis | 1879620 (61.8) | 89777 (85.3) | < 0.001a |
| Previous history of MI | 2500606 (82.3) | 16972 (16.1) | < 0.001a |
| Family history of CAD | 359298 (11.8) | 8442 (8.0) | < 0.001a |
| Previous PCI | 298852 (9.8) | 18591 (17.7) | < 0.001a |
| Previous CABG | 439722 (14.5) | 13165 (12.5) | < 0.001a |
| Previous history of cardiac arrest | 247161 (8.1) | 405 (0.4) | 0.786 |
| Smoking | 11543 (0.4) | 34019 (32.3) | < 0.001a |
| History of venous thromboembolism | 1210142 (39.8) | 3146 (3.0) | < 0.001a |
| Chronic kidney disease | 66017 (2.2) | 47909 (45.5) | < 0.001a |
| Dialysis status | 576268 (19.0) | 4388 (4.2) | < 0.001a |
| Outcomes | ACS + no gout(n = 3039546) | ACS + gout(n = 105198) | P value |
| Revascularization | |||
| Thrombolysis | 56694 (1.9) | 1408 (1.3) | < 0.001a |
| PCI | 1369759 (45.1) | 38301 (36.4) | < 0.001a |
| CABG | 245983 (8.1) | 9657 (9.2) | < 0.001a |
| All-cause in-hospital mortality | 151213 (5.0) | 4539 (4.3) | < 0.001a |
| Disposition | < 0.001a | ||
| Routine | 1878724 (61.8) | 59605 (56.7) | |
| Transfer to short-term hospital | 290145 (9.6) | 10506 (10.0) | |
| Other transfers (SNF, ICF, other) | 367183 (12.1) | 15586 (14.8) | |
| Home Health Care | 318501 (10.5) | 14208 (13.5) | |
| Against Medical Advice | 30531 (1.0) | 681 (0.6) | |
| Length of stay (d) mean (± SD) | 4.5 (± 5.2) | 5.1 (± 5.0) | < 0.001a |
| Hospital charges ($) mean (± SD) | 71312.73 (± 85186.10) | 72328.21 (± 86223.92) | < 0.001a |
We identified 3144744 ACS-related hospitalizations during the study period, of whom 3.34% (n = 105198) also had gout as comorbidity (Table 1). Patients with gout were older with more than two-thirds being > 65 years old (mean age 71.3 years), white (71.8%), mostly males (74%), and Medicare enrollees (69.1%). Interestingly, the ACS-gout cohort consisted of comparatively higher median household income population (76-100th percentile: 21.9% vs 19.1%, P < 0.001), and were more likely to be admitted to urban-teaching (54.3% vs 50.5%, P < 0.001) and Southern region hospitals (20.6% vs 17.7%, P < 0.001) as compared to those without gout. The majority (94.1%) of admissions was non-elective, and 74.4% of admissions occurred on the weekdays. As compared to ACS patients without gout, those with gout had a higher prevalence of baseline comorbidities, except CHF and previous history of cardiac arrest (Table 2). The ACS-gout patients had higher frequency of traditional comorbid risk factors such as: hypertension (83.3% vs 71.4%, P < 0.001), dyslipidemia (71.0% vs 61.8%, P < 0.001), diabetes (46.7% vs 36.6%, P < 0.001), and obesity (21.9% vs 14.6%, P < 0.001). They also had the higher prevalence of chronic kidney disease (45.5% vs 19.0%, P < 0.001), AKI (45% vs 18.7%, P < 0.001), and deficiency anemias (26.7% vs 16.0%, P < 0.001).
As shown in Table 2, the ACS patients with gout had a higher rate of undergoing CABG (9.2% vs 8.1%, P < 0.001) as compared to those without gout. All-cause in-hospital mortality associated with revascularization was lower in the ACS patients with gout compared to those without gout (4.3% vs 5.0%, P < 0.001). Gout patients were more likely to be discharged to skilled nursing facilities, intermediate care facility or similar facilities (14.8% vs 12.1%, P < 0.001) and were less likely to be discharged routinely (56.7% vs 61.8%, P < 0.001). The average LOS was higher (5.1 d vs 4.5 d, P < 0.001) and mean total hospital charges were higher ($72328 vs $71312, P < 0.001) for ACS patients with gout compared to those without gout (Table 3).
The ACS-gout cohort undergoing PCI or CABG demonstrated a higher number of postoperative complications including cardiovascular, respiratory, stroke, hemorrhage, hypotension/shock, need of blood transfusion, AKI requiring dialysis, and gastrointestinal and urinary complications as compared to those without gout (Table 3). However, overall in-hospital mortality was lower (2.2% vs 3.0%, P < 0.001) in patients with gout and there were no significant differences in the post-revascularization myocardial infarction and infection rates between both the cohorts. We also confirmed the comparable results with a comprehensive propensity-score matched analysis (Supplementary Tables 2 and 3).
On multivariable analysis, advanced age (> 85 years vs 18-44 years: OR 15.63, 95%CI: 5.51-44.39; P < 0.001), non-elective admissions (OR 2.00, 95%CI: 1.44-2.79; P < 0.001), and lower household income (OR 1.44; 95%CI: 1.17-1.78; P < 0.001) had significantly higher odds of in-hospital mortality in ACS patients with gout undergoing PCI or CABG (Table 4). Among ACS-gout cohort, Hispanics (OR 0.45, CI: 0.31-0.67; P < 0.001) and Asians (OR 0.65, CI: 0.45-0.94; P < 0.001) undergoing PCI or CABG demonstrated significantly lower odds of in-hospital mortality as compared to whites (Table 5). Rheumatoid arthritis/collagen vascular diseases, valvular heart diseases, CHF, fluid and electrolyte disorders, coagulopathy, drug abuse, neurological disorders, peripheral vascular disorders, and renal failure independently predicted a greater risk of in-hospital mortality. Additionally, ACS-gout cohort undergoing PCI or CABG revealed highest odds of in-hospital mortality due to postoperative infections followed by hypotension/shock, postoperative myocardial infarction, and postoperative stroke, respiratory, AKI, and cardiac complications.
| Complications | No gout(n = 1592156) | Gout(n = 47307) | P value |
| All-cause in-hospital mortality | 47466 (3.0) | 1038 (2.2) | < 0.001a |
| Hemorrhage | 43541 (2.7) | 1470 (3.1) | < 0.001a |
| Blood transfusion | 12272 (0.8) | 524 (1.1) | < 0.001a |
| Hypotension/shock | 7319 (0.5) | 261 (0.6) | 0.004a |
| Cardiac complications | 46511 (2.9) | 1523 (3.2) | < 0.001a |
| Postoperative myocardial infarction | 27176 (1.7) | 798 (1.7) | 0.74 |
| Stroke | 3926 (0.2) | 140 (0.3) | 0.033a |
| Respiratory complications | 46531 (2.9) | 1642 (3.5) | < 0.001a |
| Gastrointestinal complications | 25573 (1.6) | 980 (2.1) | < 0.001a |
| AKI requiring dialysis | 7843 (0.5) | 628 (1.3) | < 0.001a |
| Urinary complications | 4641 (0.3) | 307 (0.6) | < 0.001a |
| Post procedural infections | 24473 (1.5) | 687 (1.5) | 0.139 |
| Predictor | Adjusted odds ratio | 95%CI (LL-UL) | P value |
| Age in years at admission | < 0.001a | ||
| 45-64 vs 18-44 | 2.99 | 1.08-8.30 | 0.036a |
| 65-84 vs 18-44 | 5.72 | 2.04-16.01 | 0.001a |
| ≥ 85 vs 18-44 | 15.63 | 5.51-44.39 | < 0.001a |
| Male vs female | 0.89 | 0.75-1.05 | 0.155 |
| Race | < 0.001a | ||
| African American vs white | 1.09 | 0.88-1.35 | 0.413 |
| Hispanic vs white | 0.45 | 0.31-0.67 | < 0.001a |
| Asian vs white | 0.65 | 0.45-0.94 | 0.022a |
| Non-elective vs elective admission | 2.00 | 1.44-2.79 | < 0.001a |
| Median household income quartile 0-25thvs 76-100th# | 1.44 | 1.17-1.78 | 0.001a |
| Comorbidities | |||
| Alcohol abuse | 0.49 | 0.31-0.79 | 0.003a |
| Rheumatoid arthritis/collagen vascular diseases | 1.57 | 1.09-2.25 | 0.016a |
| Congestive heart failure | 5.91 | 3.54-9.86 | 0.000a |
| Coagulopathy | 1.29 | 1.05-1.58 | 0.014a |
| Drug abuse | 2.33 | 1.34-4.05 | 0.003a |
| Fluid and electrolyte disorders | 2.88 | 2.49-3.35 | < 0.001a |
| Other neurological disorders | 1.72 | 1.33-2.23 | < 0.001a |
| Obesity | 0.79 | 0.66-0.95 | 0.012a |
| Peripheral vascular disorders | 1.60 | 1.36-1.88 | < 0.001a |
| Renal failure | 2.04 | 1.13-3.70 | 0.019a |
| Valvular disease | 8.15 | 3.87-17.15 | < 0.001a |
| Dyslipidemia | 0.63 | 0.54-0.72 | < 0.001a |
| Outcomes/postoperative complications | |||
| Hypotension/shock | 2.97 | 1.93-4.56 | < 0.001a |
| Cardiac complications | 1.59 | 1.19-2.11 | 0.002a |
| Postoperative myocardial infarction | 2.53 | 1.74-3.68 | < 0.001a |
| Perioperative stroke | 2.48 | 1.20-5.10 | 0.014a |
| Respiratory complications | 1.80 | 1.41-2.30 | < 0.001a |
| Postoperative acute kidney injury | 1.48 | 1.26-1.74 | < 0.001a |
| Infections/septicemia | 3.94 | 3.01-5.16 | < 0.001a |
This is the first large scale study that evaluates the impact of gout on in-patient mortality in ACS patients and post-revascularization outcomes, predictors of in-hospital mortality during the post-revascularization period and healthcare resource utilization using the largest nationally representative cohort of ACS hospitalizations.
We found that ACS hospitalizations with gout comprised of older white men with a higher median household income, mostly Medicare beneficiaries, and were likely to be admitted to urban-teaching and Southern region hospitals more frequently. These patients also had a higher prevalence of comorbidities. Furthermore, the average LOS and total hospitalization charges were significantly higher. ACS patients with gout underwent CABG more often whereas the PCI revascularizations were comparable between both the cohorts. Those who underwent revascularizations (PCI or CABG) had shown higher overall complications; however lower all-cause in-hospital mortality compared to those without gout. A multivariate analysis demonstrated that older age, Hispanic and Asian race, lower household income, non-elective admi-ssions, a previous history of CHF, valvular diseases, septicemia, shock, and cardiovascular complications were independent predictors of in-hospital mortality in ACS hospitalizations with gout post-revascularization.
In the study, the prevalence of gout among ACS patients was about 3.35% similar to the prevalence of gout among healthy United States population to be 3%-5%, with the age-standardized prevalence of hyperuricemia being 12%-15%[16]. In this study, gout has been prevalent in ACS patients with lower all-cause mortality compared to without gout. More recently, Latif et al[17] indicated that higher UA levels are associated with lower all-cause and cardiovascular mortality, however, they included only hemodialysis patients. Similarly, another study using the NIS suggested that co-occurring gout is associated with reduced in-hospital mortality among postmeno-pausal women admitted for AMI[18]. The paradoxical association with mortality could be due to focus on the short-term post-revascularization in-hospital outcomes, residual confounding factors in administrative data, or missed diagnosis in patients without gout. As shown with previous studies, our findings also showed that ACS hospitalizations with gout consisted of older white men, with higher co-existing comorbid conditions, mostly Medicare enrollees, and a lower median income quartile[19-21]. Surprisingly, Harrold et al[22] found that older women with gout more often had coronary heart disease. The results of our study suggest that ACS patients with gout had prolonged hospital stays post-revascularizations and management costs. A few other studies have also confirmed similar findings[23,24]. These studies have given a possible explanation for a prolonged stay and increased hospital cost due to increased risk of recurrent events and complications; however, the results were limited to the economic impact of ACS in general. This would be one of the few studies to describe the impact of gout on outcomes of ACS hospitalizations in terms of healthcare resource utilization including revascularization, the ensuing economic impact and the predictors of post-revascularization inpatient mortality.
We found that age, race, median income, relevant comorbidities, and post-revascularization outcomes/postoperative complications in ACS patients undergoing PCI or CABG were independently predictive of in-hospital mortality in ACS patients with gout. Conversely, no association was observed in gender, which is consistent with a previous meta-analysis[25]. The gender-specific relative risk for congestive heart diseases (CHD) in that metanalysis for each increase of 1 mg/dL in serum UA was similar, but not statistically significant. However, subgroup analysis showed a significant association between hyperuricemia and CHD incidence in men, but increased risk of CHD mortality in women. The result differs from the previous studies that showed both men and women with gout have increased the risk of cardiovascular mortality compared with those without gout[26-28]. A retrospective study of STEMI patients who underwent PCI reported that one in every five patients had higher UA levels and it was independently associated with increased risk of in-hospital mortality[10]. Ndrepepa et al[29] reported that every 1 mg/dL rise in UA increased by 12% in the adjusted risk for 1-year mortality in an unselected cohort. Alcohol consumption and dyslipidemia have been associated with significantly increase the risk of hyperuricemia[30,31], which could further precipitate or increase the severity of gout. Interestingly, we observed the lower odds of in-hospital mortality with alcohol abuse, dyslipidemia, and obesity in ACS patients with gout undergoing revascularization. The implication of our findings is important for targeted preventive intervention in a certain population at the risk of gout and ACS.
Several potential mechanisms including causal role of UA in hypertension and atherosclerosis development, vasoconstriction, role of UA as pro-oxidant or gout per se promoting atherosclerosis, explain the increased risk of cardiovascular mortality in patients with gout[32,33]. However, whether gout is an independent factor with a pathogenic role in ACS or only attributing for associated risk factors of ACS, such as obesity, renal diseases, and diabetes, remains debatable[26,34]. In several large sample studies, gout was linked to increased all-cause and CV mortality rates[28,35,36], nonetheless, data on the impact of gout on post-revascularization remains limited in the literature.
Our study extends on the impact of gout on ACS patients with other comorbid conditions and revascularization complications. The study showed that cardiac, renal, pulmonary and vascular comorbidities are the risk factors for post-revascularization complications as well. Previous studies have shown an association of gout and hype-ruricemia with many comorbid conditions. Demir et al[37] showed increased serum UA levels in calcific aortic valve stenosis (AS), with a positive correlation in the severity of the disease. Raised serum UA level may initiate calcification in the aortic valve and accelerate the progression by causing endothelial dysfunction[32]. Similarly, a prospective longitudinal study with a large cohort of 11681 men also concluded that CHF decompensation is independently associated with increased risk of hyperuricemia and likely gout, by increased urate production and decreased renal urate excretion[38]. Our study also shows an increased risk of in-hospital mortality in ACS patients with gout who are drug abusers that have never been evaluated in the past.
Systemic (kidney, respiratory and vascular) complications of revascularization in ACS patients with gout were likely to increase in-hospital mortality compared to patients without gout. This could also be the reason for prolonged hospitalization and increased treatment cost. Ejaz et al[39] showed that the UA is associated with a five to eight-fold increase in the post-cardiac surgery AKI. A study from the United Kingdom found 1.71 times higher risk of stroke in patients with gout than in the general population[40]. A nationwide population-based cohort study showed that gout was associated with an increased risk of pulmonary embolism by almost 53%[41]. Several studies have shown an association between gout and collagen vascular diseases, such as systemic sclerosis and rheumatoid arthritis[42,43]. Our findings would be prospective to initiate the discussion of screening and appropriate treatment of gout in ACS patients, and other dynamics responsible for gout should be considered when targeting new therapeutic strategies to prevent postoperative complications. In addition, appropriate screening for CVD in patients with gout is suggested as these patients have worse cardiovascular outcomes.
Our retrospective database study has few limitations which need to be mentioned. Due to the administrative nature of this database, some baseline patient’s data might be missing, and follow up data was not available. There is a possibility of a misclassi-fication bias from the use of diagnostic codes to define gout based on the clinical findings by physicians or to diagnose ACS, with a possible change in terminology and use of generalized diagnostic codes by the clinicians. The NIS database does not contain information on serum uric acid level in gout patients so the severity and the extent of worse outcomes in ACS and post-revascularization outcomes with a unit increase in uric acid levels are not possible to be evaluated. In addition, each hospitalization is considered separately in the NIS, which could result in overestimation of the number of admissions for the same patient. Furthermore, the study emphasizes the short-term in-hospital impact of gout, lacking long-term follow-up outcomes. Nevertheless, the current study showed several important strengths, including nationwide large sample size, standardized methods, and absence of selection bias.
In conclusion, although gout did not increase the in-hospital mortality in ACS-related hospitalizations, the findings from this nationwide cohort highlight the significant impact of gout on in-hospital outcomes in ACS patients in terms of higher cardiovascular comorbidities, CABG frequency, post-revascularization complications, hospital stay, and total hospital charges.
Previous studies have established a role of gout in predicting risk and prognosis of cardiovascular diseases. However, large-scale data on the impact of gout on inpatient outcomes of acute coronary syndrome (ACS)-related hospitalizations and post-revascularization is inadequate.
Limited data exist on impact of gout on in-hospital outcome of ACS in terms of healthcare utilization and post-revascularization outcomes.
The study aimed to evaluate the impact of gout on in-hospital outcomes of ACS hospitalizations, subsequent healthcare burden and predictors of post-revascularization inpatient mortality.
We used the national inpatient sample (2010-2014) to identify the ACS and gout-related hospitalizations, relevant comorbidities, revascularization and post-revascularization outcomes using the ICD-9 CM codes. A multivariable analysis was performed to evaluate the predictors of post-revascularization in-hospital mortality.
Out of 3144744 ACS-related hospitalizations, 105198 (3.35%) patients had gout. The ACS-gout cohort were more often older white males with a higher prevalence of comorbidities. ACS-gout cohort showed comparativly higher prevalence of Coronary artery bypass grafting. Post-revascularization complications including cardiac (3.2% vs 2.9%), respiratory (3.5% vs 2.9%), and hemorrhage (3.1% vs 2.7%) were higher whereas all-cause mortality was lower (2.2% vs 3.0%) in the ACS-gout cohort (P < 0.001). An older age (OR 15.63, CI: 5.51-44.39), non-elective admissions (OR 2.00, CI: 1.44-2.79), lower household income (OR 1.44; CI: 1.17-1.78), and comorbid conditions predicted higher mortality in ACS-gout cohort undergoing revascularization (P < 0.001). Odds of post-revascularization in-hospital mortality were lower in Hispanics (OR 0.45, CI: 0.31-0.67) and Asians (OR 0.65, CI: 0.45-0.94) as compared to white (P < 0.001). However, post-operative complications significantly raised mortality odds. Mean length of stay, transfer to other facilities, and hospital charges were higher in the ACS-gout cohort.
Gout was not independently associated with an increased risk of post-revascularization in-hospital mortality in ACS. However, gout did increase post-revascularization complications.
This study may help clinicians making evidence-based decision in patients with history of gout who are admitted with primary diagnosis of ACS and have undergone re-vascularization.
Manuscript source: Unsolicited manuscript
Specialty type: Cardiac and cardiovascular systems
Country of origin: United States
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| 1. | Kumar A, Cannon CP. Acute coronary syndromes: diagnosis and management, part I. Mayo Clin Proc. 2009;84:917-938. [PubMed] [DOI] [Cited in This Article: ] [Cited by in F6Publishing: 109] [Reference Citation Analysis (0)] |
| 2. | Granger CB, Goldberg RJ, Dabbous O, Pieper KS, Eagle KA, Cannon CP, Van De Werf F, Avezum A, Goodman SG, Flather MD, Fox KA; Global Registry of Acute Coronary Events Investigators. Predictors of hospital mortality in the global registry of acute coronary events. Arch Intern Med. 2003;163:2345-2353. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1444] [Cited by in F6Publishing: 1533] [Article Influence: 73.0] [Reference Citation Analysis (0)] |
| 3. | Fox KA, Goodman SG, Anderson FA, Granger CB, Moscucci M, Flather MD, Spencer F, Budaj A, Dabbous OH, Gore JM; GRACE Investigators. From guidelines to clinical practice: the impact of hospital and geographical characteristics on temporal trends in the management of acute coronary syndromes. The Global Registry of Acute Coronary Events (GRACE). Eur Heart J. 2003;24:1414-1424. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 176] [Cited by in F6Publishing: 194] [Article Influence: 9.2] [Reference Citation Analysis (0)] |
| 4. | Singh G, Mithal A, Mithal A. THU0409 Not just a swollen big toe: increasing all-cause hospitalizations in patients with gout in the United States: 1993-2014. Ann Rheum Dis. 2017;76:362. [DOI] [Cited in This Article: ] |
| 5. | Chapman PT, Yarwood H, Harrison AA, Stocker CJ, Jamar F, Gundel RH, Peters AM, Haskard DO. Endothelial activation in monosodium urate monohydrate crystal-induced inflammation: in vitro and in vivo studies on the roles of tumor necrosis factor alpha and interleukin-1. Arthritis Rheum. 1997;40:955-965. [PubMed] [DOI] [Cited in This Article: ] [Cited by in F6Publishing: 1] [Reference Citation Analysis (0)] |
| 6. | Borghi C, Cicero AFG. Serum uric acid and acute coronary syndrome: Is there a role for functional markers of residual cardiovascular risk? Int J Cardiol. 2018;250:62-63. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis (0)] |
| 7. | Lottmann K, Chen X, Schädlich PK. Association between gout and all-cause as well as cardiovascular mortality: a systematic review. Curr Rheumatol Rep. 2012;14:195-203. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 60] [Cited by in F6Publishing: 64] [Article Influence: 5.3] [Reference Citation Analysis (0)] |
| 8. | Bickel C, Rupprecht HJ, Blankenberg S, Rippin G, Hafner G, Daunhauer A, Hofmann KP, Meyer J. Serum uric acid as an independent predictor of mortality in patients with angiographically proven coronary artery disease. Am J Cardiol. 2002;89:12-17. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 150] [Cited by in F6Publishing: 146] [Article Influence: 6.6] [Reference Citation Analysis (0)] |
| 9. | Magnoni M, Berteotti M, Ceriotti F, Mallia V, Vergani V, Peretto G, Angeloni G, Cristell N, Maseri A, Cianflone D. Serum uric acid on admission predicts in-hospital mortality in patients with acute coronary syndrome. Int J Cardiol. 2017;240:25-29. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 42] [Cited by in F6Publishing: 45] [Article Influence: 6.4] [Reference Citation Analysis (0)] |
| 10. | Lazzeri C, Valente S, Chiostri M, Sori A, Bernardo P, Gensini GF. Uric acid in the acute phase of ST elevation myocardial infarction submitted to primary PCI: its prognostic role and relation with inflammatory markers: a single center experience. Int J Cardiol. 2010;138:206-209. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 81] [Cited by in F6Publishing: 89] [Article Influence: 5.6] [Reference Citation Analysis (0)] |
| 11. | Kittleson MM, Bead V, Fradley M, St John ME, Champion HC, Kasper EK, Russell SD, Wittstein IS, Hare JM. Elevated uric acid levels predict allograft vasculopathy in cardiac transplant recipients. J Heart Lung Transplant. 2007;26:498-503. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 0.6] [Reference Citation Analysis (0)] |
| 12. | Morishima I, Sone T, Mokuno S, Taga S, Shimauchi A, Oki Y, Kondo J, Tsuboi H, Sassa H. Clinical significance of no-reflow phenomenon observed on angiography after successful treatment of acute myocardial infarction with percutaneous transluminal coronary angioplasty. Am Heart J. 1995;130:239-243. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 137] [Cited by in F6Publishing: 142] [Article Influence: 4.9] [Reference Citation Analysis (0)] |
| 13. | Morishima I, Sone T, Okumura K, Tsuboi H, Kondo J, Mukawa H, Matsui H, Toki Y, Ito T, Hayakawa T. Angiographic no-reflow phenomenon as a predictor of adverse long-term outcome in patients treated with percutaneous transluminal coronary angioplasty for first acute myocardial infarction. J Am Coll Cardiol. 2000;36:1202-1209. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 399] [Cited by in F6Publishing: 414] [Article Influence: 17.3] [Reference Citation Analysis (0)] |
| 14. | Healthcare Cost and Utilization Project. Overview of the National (Nationwide) Inpatient Sample (NIS). Available from: https://www.hcup-us.ahrq.gov/nisoverview.jsp. [Cited in This Article: ] |
| 15. | Elgendy IY, Mahmoud AN, Mansoor H, Bavry AA. Early Invasive Versus Initial Conservative Strategies for Women with Non-ST-Elevation Acute Coronary Syndromes: A Nationwide Analysis. Am J Med. 2017;130:1059-1067. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 24] [Cited by in F6Publishing: 18] [Article Influence: 2.6] [Reference Citation Analysis (0)] |
| 16. | Chen-Xu M, Yokose C, Choi HK. SAT0703 Racial disparities in gout and hyperuricemia - a united states general population study. Ann Rheum Dis. 2018;77:1199-200. [DOI] [Cited in This Article: ] |
| 17. | Latif W, Karaboyas A, Tong L, Winchester JF, Arrington CJ, Pisoni RL, Marshall MR, Kleophas W, Levin NW, Sen A, Robinson BM, Saran R. Uric acid levels and all-cause and cardiovascular mortality in the hemodialysis population. Clin J Am Soc Nephrol. 2011;6:2470-2477. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 104] [Cited by in F6Publishing: 95] [Article Influence: 7.3] [Reference Citation Analysis (0)] |
| 18. | Adegbala O, Adejumo AC, Olakanmi O, Akinjero A, Akintoye E, Alliu S, Edo-Osagie E, Chatterjee A. Relation of Cannabis Use and Atrial Fibrillation Among Patients Hospitalized for Heart Failure. Am J Cardiol. 2018;122:129-134. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 17] [Cited by in F6Publishing: 20] [Article Influence: 3.3] [Reference Citation Analysis (0)] |
| 19. | Pagidipati NJ, Hess CN, Clare RM, Akerblom A, Tricoci P, Wojdyla D, Keenan RT, James S, Held C, Mahaffey KW, Klein AB, Wallentin L, Roe MT. An examination of the relationship between serum uric acid level, a clinical history of gout, and cardiovascular outcomes among patients with acute coronary syndrome. Am Heart J. 2017;187:53-61. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 27] [Cited by in F6Publishing: 26] [Article Influence: 3.7] [Reference Citation Analysis (0)] |
| 20. | Pillinger MH, Bangalore S, Klein AB, Baumgartner S, Morlock R. Cardiovascular Disease and Gout: Real-World Experience Evaluating Patient Characteristics, Treatment Patterns, and Health Care Utilization. J Manag Care Spec Pharm. 2017;23:677-683. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis (0)] |
| 21. | Singh JA, Yu S. Gout-related inpatient utilization: a study of predictors of outcomes and time trends. Arthritis Res Ther. 2016;18:57. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.4] [Reference Citation Analysis (0)] |
| 22. | Harrold LR, Yood RA, Mikuls TR, Andrade SE, Davis J, Fuller J, Chan KA, Roblin D, Raebel MA, Von Worley A, Platt R, Saag KG. Sex differences in gout epidemiology: evaluation and treatment. Ann Rheum Dis. 2006;65:1368-1372. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 102] [Cited by in F6Publishing: 106] [Article Influence: 5.9] [Reference Citation Analysis (0)] |
| 23. | Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Makuc DM, Marcus GM, Marelli A, Matchar DB, Moy CS, Mozaffarian D, Mussolino ME, Nichol G, Paynter NP, Soliman EZ, Sorlie PD, Sotoodehnia N, Turan TN, Virani SS, Wong ND, Woo D, Turner MB; American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Heart disease and stroke statistics--2012 update: a report from the American Heart Association. Circulation. 2012;125:e2-e220. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2378] [Cited by in F6Publishing: 3163] [Article Influence: 263.6] [Reference Citation Analysis (0)] |
| 24. | LaMori JC, Shoheiber O, Dudash K, Crivera C, Mody SH. The economic impact of acute coronary syndrome on length of stay: an analysis using the Healthcare Cost and Utilization Project (HCUP) databases. J Med Econ. 2014;17:191-197. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 17] [Cited by in F6Publishing: 25] [Article Influence: 2.5] [Reference Citation Analysis (0)] |
| 25. | Kim SY, Guevara JP, Kim KM, Choi HK, Heitjan DF, Albert DA. Hyperuricemia and coronary heart disease: a systematic review and meta-analysis. Arthritis Care Res (Hoboken). 2010;62:170-180. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 80] [Cited by in F6Publishing: 252] [Article Influence: 18.0] [Reference Citation Analysis (0)] |
| 26. | Choi HK, Curhan G. Independent impact of gout on mortality and risk for coronary heart disease. Circulation. 2007;116:894-900. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 431] [Cited by in F6Publishing: 439] [Article Influence: 25.8] [Reference Citation Analysis (0)] |
| 27. | Krishnan E, Svendsen K, Neaton JD, Grandits G, Kuller LH; MRFIT Research Group. Long-term cardiovascular mortality among middle-aged men with gout. Arch Intern Med. 2008;168:1104-1110. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 246] [Cited by in F6Publishing: 262] [Article Influence: 16.4] [Reference Citation Analysis (1)] |
| 28. | De Vera MA, Rahman MM, Bhole V, Kopec JA, Choi HK. Independent impact of gout on the risk of acute myocardial infarction among elderly women: a population-based study. Ann Rheum Dis. 2010;69:1162-1164. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 96] [Cited by in F6Publishing: 98] [Article Influence: 7.0] [Reference Citation Analysis (0)] |
| 29. | Ndrepepa G, Braun S, Haase HU, Schulz S, Ranftl S, Hadamitzky M, Mehilli J, Schömig A, Kastrati A. Prognostic value of uric acid in patients with acute coronary syndromes. Am J Cardiol. 2012;109:1260-1265. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 52] [Cited by in F6Publishing: 61] [Article Influence: 5.1] [Reference Citation Analysis (0)] |
| 30. | Li Z, Guo X, Liu Y, Chang Y, Sun Y, Zhu G, Abraham MR. The Relation of Moderate Alcohol Consumption to Hyperuricemia in a Rural General Population. Int J Environ Res Public Health. 2016;13:pii: E732. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 13] [Cited by in F6Publishing: 17] [Article Influence: 2.1] [Reference Citation Analysis (0)] |
| 31. | Peng TC, Wang CC, Kao TW, Chan JY, Yang YH, Chang YW, Chen WL. Relationship between hyperuricemia and lipid profiles in US adults. Biomed Res Int. 2015;2015:127596. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 86] [Cited by in F6Publishing: 126] [Article Influence: 14.0] [Reference Citation Analysis (0)] |
| 32. | Kanellis J, Kang DH. Uric acid as a mediator of endothelial dysfunction, inflammation, and vascular disease. Semin Nephrol. 2005;25:39-42. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 270] [Cited by in F6Publishing: 279] [Article Influence: 14.7] [Reference Citation Analysis (0)] |
| 33. | Feig DI, Kang DH, Johnson RJ. Uric acid and cardiovascular risk. N Engl J Med. 2008;359:1811-1821. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1599] [Cited by in F6Publishing: 1730] [Article Influence: 108.1] [Reference Citation Analysis (0)] |
| 34. | Johnson RJ, Kang DH, Feig D, Kivlighn S, Kanellis J, Watanabe S, Tuttle KR, Rodriguez-Iturbe B, Herrera-Acosta J, Mazzali M. Is there a pathogenetic role for uric acid in hypertension and cardiovascular and renal disease? Hypertension. 2003;41:1183-1190. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 860] [Cited by in F6Publishing: 884] [Article Influence: 42.1] [Reference Citation Analysis (0)] |
| 35. | Kuo CF, See LC, Luo SF, Ko YS, Lin YS, Hwang JS, Lin CM, Chen HW, Yu KH. Gout: an independent risk factor for all-cause and cardiovascular mortality. Rheumatology (Oxford). 2010;49:141-146. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 156] [Cited by in F6Publishing: 151] [Article Influence: 10.1] [Reference Citation Analysis (0)] |
| 36. | Stack AG, Hanley A, Casserly LF, Cronin CJ, Abdalla AA, Kiernan TJ, Murthy BV, Hegarty A, Hannigan A, Nguyen HT. Independent and conjoint associations of gout and hyperuricaemia with total and cardiovascular mortality. QJM. 2013;106:647-658. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 100] [Cited by in F6Publishing: 102] [Article Influence: 9.3] [Reference Citation Analysis (0)] |
| 37. | Demir B, Caglar IM, Ugurlucan M, Ozde C, Tureli HO, Cifci S, Vural A, Karakaya O. The relationship between severity of calcific aortic stenosis and serum uric acid levels. Angiology. 2012;63:603-608. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 1.2] [Reference Citation Analysis (0)] |
| 38. | Misra D, Zhu Y, Zhang Y, Choi HK. The independent impact of congestive heart failure status and diuretic use on serum uric acid among men with a high cardiovascular risk profile: a prospective longitudinal study. Semin Arthritis Rheum. 2011;41:471-476. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 1.2] [Reference Citation Analysis (0)] |
| 39. | Ejaz AA, Kambhampati G, Ejaz NI, Dass B, Lapsia V, Arif AA, Asmar A, Shimada M, Alsabbagh MM, Aiyer R, Johnson RJ. Post-operative serum uric acid and acute kidney injury. J Nephrol. 2012;25:497-505. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 32] [Cited by in F6Publishing: 35] [Article Influence: 2.9] [Reference Citation Analysis (0)] |
| 40. | Seminog OO, Goldacre MJ. Gout as a risk factor for myocardial infarction and stroke in England: evidence from record linkage studies. Rheumatology (Oxford). 2013;52:2251-2259. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 62] [Cited by in F6Publishing: 64] [Article Influence: 5.8] [Reference Citation Analysis (0)] |
| 41. | Huang CC, Huang PH, Chen JH, Lan JL, Tsay GJ, Lin HY, Tseng CH, Lin CL, Hsu CY. An Independent Risk of Gout on the Development of Deep Vein Thrombosis and Pulmonary Embolism: A Nationwide, Population-Based Cohort Study. Medicine (Baltimore). 2015;94:e2140. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.7] [Reference Citation Analysis (0)] |
| 42. | Gigante A, Barbano B, Barilaro G, Quarta S, Gasperini ML, Di Mario F, Romaniello A, Amoroso A, Cianci R, Rosato E. Serum uric acid as a marker of microvascular damage in systemic sclerosis patients. Microvasc Res. 2016;106:39-43. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 1.8] [Reference Citation Analysis (0)] |
| 43. | Jebakumar AJ, Udayakumar PD, Crowson CS, Matteson EL. Occurrence of gout in rheumatoid arthritis: it does happen! A population-based study. Int J Clin Rheumtol. 2013;8:433-437. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis (0)] |